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D M Layton

Showing results (31-40 of 51) with videos related to

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Blood|June 1, 1996
Prenatal diagnosis of triosephosphate isomerase deficiencyR Arya, M R Lalloz, K H Nicolaides, et al.
Fetal Diagnosis and Therapy|July 1, 1993
Fetal plasma tumor necrosis factor concentration in normal pregnancyA Abbas, R J Snijders, A G Buggins, et al.
American Journal of Hematology|July 31, 2013
Diagnosis of pyrimidine 5'-nucleotidase deficiency suspected from a blood filmHassan A Al-Jafar, D M Layton, Lynn Robertson, et al.
British Journal of Haematology|April 1, 1989
Myelofibrosis in primary myelodysplastic syndromes: a clinico-morphological study of 10 casesA Pagliuca, D M Layton, A Manoharan, et al.
Lancet (London, England)|April 21, 1999
Towards enzyme-replacement treatment in triosephosphate isomerase deficiencyA Ationu, A Humphries, B Wild, et al.
International Journal of Molecular Medicine|December 19, 1998
Quantification of Ggamma- and Agamma-globins by electrospray ionisation mass spectrometryS F Ofori-Acquah, B N Green, B J Wild, et al.
Blood|October 15, 1996
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemiaJ Manabe, R Arya, H Sumimoto, et al.
Obstetric Medicine|September 1, 2016
Pregnancy outcomes in sickle cell disease: a retrospective cohort study from two tertiary centres in the UKA R Chase, M Sohal, J Howard, et al.
Blood Cells, Molecules & Diseases|November 29, 2005
Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infantM J Percy, L J Crowley, D Roper, et al.
Archives of Disease in Childhood|April 1, 1992
Blood leucocyte count in the human fetusN P Davies, A G Buggins, R J Snijders, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Blood|June 1, 1996
Prenatal diagnosis of triosephosphate isomerase deficiencyR Arya, M R Lalloz, K H Nicolaides, et al.
Fetal Diagnosis and Therapy|July 1, 1993
Fetal plasma tumor necrosis factor concentration in normal pregnancyA Abbas, R J Snijders, A G Buggins, et al.
American Journal of Hematology|July 31, 2013
Diagnosis of pyrimidine 5'-nucleotidase deficiency suspected from a blood filmHassan A Al-Jafar, D M Layton, Lynn Robertson, et al.
British Journal of Haematology|April 1, 1989
Myelofibrosis in primary myelodysplastic syndromes: a clinico-morphological study of 10 casesA Pagliuca, D M Layton, A Manoharan, et al.
Lancet (London, England)|April 21, 1999
Towards enzyme-replacement treatment in triosephosphate isomerase deficiencyA Ationu, A Humphries, B Wild, et al.
International Journal of Molecular Medicine|December 19, 1998
Quantification of Ggamma- and Agamma-globins by electrospray ionisation mass spectrometryS F Ofori-Acquah, B N Green, B J Wild, et al.
Blood|October 15, 1996
Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemiaJ Manabe, R Arya, H Sumimoto, et al.
Obstetric Medicine|September 1, 2016
Pregnancy outcomes in sickle cell disease: a retrospective cohort study from two tertiary centres in the UKA R Chase, M Sohal, J Howard, et al.
Blood Cells, Molecules & Diseases|November 29, 2005
Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b(5) reductase: an aid to determine recessive congenital methemoglobinemia status in an infantM J Percy, L J Crowley, D Roper, et al.
Archives of Disease in Childhood|April 1, 1992
Blood leucocyte count in the human fetusN P Davies, A G Buggins, R J Snijders, et al.
Pageof 6